Taiwan FDA registration 8ffc3cc411119acd7a10f283d239dc8a

Apollo lens corrective spectacle lens (Non-sterile) 

TW: 至尊矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·FUJITA OPTICAL CO., LTD.·Registered Sep 05, 2013 – Sep 05, 2023Expired
Registration details
Analysis ID
8ffc3cc411119acd7a10f283d239dc8a
License Form
Ministry of Health Medical Device Import No. 013388
Customs Code
DHA09401338807
Company information
Manufacturer Country
Japan
Authorized Representative
HKO OPTICAL LENS (TAIWAN) CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M5844 corrective lenses
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 05, 2013
Expiry Date
Sep 05, 2023
Companies making similar products

Top companies providing products similar to "Apollo lens corrective spectacle lens (Non-sterile) "

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for Apollo lens corrective spectacle lens (Non-sterile)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8ffc3cc411119acd7a10f283d239dc8a and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HONG KONG OPTICAL LENS CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations